glipizide

Generic: glipizide

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glipizide
Generic Name glipizide
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glipizide 5 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4857
Product ID 68071-4857_2d05cc33-c6ea-86cc-e063-6394a90a3fb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075795
Listing Expiration 2026-12-31
Marketing Start 2002-09-25

Pharmacologic Class

Established (EPC)
sulfonylurea [epc]
Chemical Structure
sulfonylurea compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714857
Hyphenated Format 68071-4857

Supplemental Identifiers

RxCUI
310490
UPC
0368071485714
UNII
X7WDT95N5C
NUI
N0000175608 M0020795

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name glipizide (source: ndc)
Generic Name glipizide (source: ndc)
Application Number ANDA075795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68071-4857-1)
source: ndc

Packages (1)

Ingredients (1)

glipizide (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d05cc33-c6ea-86cc-e063-6394a90a3fb7", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368071485714"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["86e6583c-b290-e2b5-e053-2991aa0ab485"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-4857-1)", "package_ndc": "68071-4857-1", "marketing_start_date": "20190419"}], "brand_name": "Glipizide", "product_id": "68071-4857_2d05cc33-c6ea-86cc-e063-6394a90a3fb7", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68071-4857", "generic_name": "Glipizide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20261231"}